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Author
Drouot N
Drouot N
References (2)
1. Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment - Quartier_2019_Hum.Mutat_40_2021
Title :
Novel mutations in NLGN3 causing autism spectrum disorder and cognitive impairment -
Quartier_2019_Hum.Mutat_40_2021
Author(s) :
Quartier A
,
Courraud J
,
Thi Ha T
,
McGillivray G
,
Isidor B
,
Rose K
,
Drouot N
,
Savidan MA
,
Feger C
,
Jagline H
,
Chelly J
,
Shaw M
,
Laumonnier F
,
Gecz J
,
Mandel JL
,
Piton A
Ref :
Hum Mutat ,
40
:2021 , 2019
Abstract :
View Abstract
PubMedSearch :
Quartier_2019_Hum.Mutat_40_2021
PubMedID
:
31184401
Gene_locus related to this paper:
human-NLGN3
2. Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism - Fiskerstrand_2010_Am.J.Hum.Genet_87_410
Title :
Mutations in ABHD12 cause the neurodegenerative disease PHARC: An inborn error of endocannabinoid metabolism -
Fiskerstrand_2010_Am.J.Hum.Genet_87_410
Author(s) :
Fiskerstrand T
,
H'Mida-Ben Brahim D
,
Johansson S
,
M'Zahem A
,
Haukanes BI
,
Drouot N
,
Zimmermann J
,
Cole AJ
,
Vedeler C
,
Bredrup C
,
Assoum M
,
Tazir M
,
Klockgether T
,
Hamri A
,
Steen VM
,
Boman H
,
Bindoff LA
,
Koenig M
,
Knappskog PM
Ref :
American Journal of Human Genetics ,
87
:410 , 2010
Abstract :
View Abstract
PubMedSearch :
Fiskerstrand_2010_Am.J.Hum.Genet_87_410
PubMedID
:
20797687
Gene_locus related to this paper:
human-ABHD12